Mystery solved after 23 years: M syndrome is PIGT-associated multiple congenital anomalies-hypotonia-seizures syndrome 3 (2022)
- Authors:
- Autor USP: KOK, FERNANDO - FM
- Unidade: FM
- DOI: 10.1002/ajmg.a.62977
- Subjects: CONVULSÕES; CONVULSOTERAPIA
- Language: Inglês
- Imprenta:
- Source:
- Título: American journal of medical genetics part a
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: v. 188, n. 12, p. 3567-3568, 2022
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
NOBREGA, Paulo Ribeiro et al. Mystery solved after 23 years: M syndrome is PIGT-associated multiple congenital anomalies-hypotonia-seizures syndrome 3. American journal of medical genetics part a, v. 188, n. 12, p. 3567-3568, 2022Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/50568. Acesso em: 11 nov. 2024. -
APA
Nobrega, P. R., Castro, M. A. A., Paiva, A. R. B. de, & Kok, F. (2022). Mystery solved after 23 years: M syndrome is PIGT-associated multiple congenital anomalies-hypotonia-seizures syndrome 3. American journal of medical genetics part a, 188( 12), 3567-3568. doi:10.1002/ajmg.a.62977 -
NLM
Nobrega PR, Castro MAA, Paiva ARB de, Kok F. Mystery solved after 23 years: M syndrome is PIGT-associated multiple congenital anomalies-hypotonia-seizures syndrome 3 [Internet]. American journal of medical genetics part a. 2022 ; 188( 12): 3567-3568.[citado 2024 nov. 11 ] Available from: https://observatorio.fm.usp.br/handle/OPI/50568 -
Vancouver
Nobrega PR, Castro MAA, Paiva ARB de, Kok F. Mystery solved after 23 years: M syndrome is PIGT-associated multiple congenital anomalies-hypotonia-seizures syndrome 3 [Internet]. American journal of medical genetics part a. 2022 ; 188( 12): 3567-3568.[citado 2024 nov. 11 ] Available from: https://observatorio.fm.usp.br/handle/OPI/50568 - Encefalopatias progressivas em crianças
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Informações sobre o DOI: 10.1002/ajmg.a.62977 (Fonte: oaDOI API)
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